ICD Code Hub
Получать обновления
Предстоящий1 окт. 2026 г. – 30 сент. 2027 г.
Инструменты справочника
Указатель заболеваний

Syndrome

Указатель заболеваний · Модификаторы и ссылки

Модификаторы и ссылки · icd10cm-index-2027.xml

Syndrome

MERRF(myoclonic epilepsy associated with ragged-red fibers)

E88.42

Syndrome

mesenteric

Syndrome › mesenteric

artery(superior)

K55.1

Syndrome › mesenteric

vascular insufficiency

K55.1

Syndrome

metastatic carcinoid

E34.00

Syndrome

micrognathia-glossoptosis

Q87.0

Syndrome

middle lobe(lung)

J98.19

Syndrome

middle radicular

G54.0

Syndrome

migraine

G43.909-

See also: Migraine

Syndrome

Millard-Gubler

G46.3

Syndrome

Miller-Fisher

G61.0

Syndrome

Minkowski-Chauffard

D58.0

Syndrome

MNGIE(Mitochondrial Neurogastrointestinal Encephalopathy)

E88.49

Syndrome

Möbius, ophthalmoplegic migraine

See: Migraine, ophthalmoplegic

Syndrome

Morel-Morgagni

M85.2

Syndrome

Morgagni(-Morel) (-Stewart)

M85.2

Syndrome

Morgagni-Adams-Stokes

I45.9

Syndrome

Muckle-Wells

M04.2

Syndrome

mucocutaneous lymph node(acute febrile) (MCLS)

M30.3

Syndrome

multiple endocrine neoplasia(MEN)

See: Neoplasia, endocrine, multiple (MEN)

Syndrome

multiple operations

See: Disorder, factitious

Syndrome

multisystem inflammatory(in adults) (in children)

M35.81

Syndrome

Mounier-Kuhn

Q32.4

Syndrome › Mounier-Kuhn

with bronchiectasis

J47.9

Syndrome › Mounier-Kuhn › with bronchiectasis

with

Syndrome › Mounier-Kuhn › with bronchiectasis › with

exacerbation(acute)

J47.1

Syndrome › Mounier-Kuhn › with bronchiectasis › with

lower respiratory infection

J47.0

Syndrome › Mounier-Kuhn

acquired

J98.09

Syndrome › Mounier-Kuhn › acquired

with bronchiectasis

J47.9

Syndrome › Mounier-Kuhn › acquired › with bronchiectasis

with

Syndrome › Mounier-Kuhn › acquired › with bronchiectasis › with

exacerbation(acute)

J47.1

Syndrome › Mounier-Kuhn › acquired › with bronchiectasis › with

lower respiratory infection

J47.0

Syndrome › myasthenic

in

Syndrome › myasthenic › in

diabetes mellitus

See: Diabetes, amyotrophy

Syndrome › myasthenic › in

endocrine disease NEC

E34.9

Manifestation: G73.3

Syndrome › myasthenic › in

neoplastic disease

D49.9

See also: Neoplasm

Manifestation: G73.3

Syndrome › myasthenic › in

thyrotoxicosis(hyperthyroidism)

E05.90

Manifestation: G73.3

Syndrome › myasthenic › in › thyrotoxicosis(hyperthyroidism)

with thyroid storm

E05.91

Manifestation: G73.3

Syndrome

myelodysplastic

D46.9

Syndrome › myelodysplastic

with

Syndrome › myelodysplastic › with

5q deletion

D46.C

Syndrome › myelodysplastic › with

isolated del(5q) chromosomal abnormality

D46.C

Syndrome › myelodysplastic › with

multilineage dysplasia

D46.A

Syndrome › myelodysplastic › with › multilineage dysplasia

with ringed sideroblasts

D46.B

Syndrome › myelodysplastic › with

pancytopenia(acquired)

D61.818

Syndrome › myelodysplastic

lesions, low grade

D46.20

Syndrome › myelodysplastic

specified NEC

D46.Z

Syndrome

myeloid hypereosinophilic

D72.118

Syndrome

myelopathic pain

G89.0

Syndrome

myeloproliferative(chronic)

D47.1

Syndrome

nail patella

Q87.2

Syndrome

NARP(Neuropathy, Ataxia and Retinitis pigmentosa)

E88.49

Syndrome

neonatal abstinence

P96.1

Syndrome

nephritic

See also: Nephritis

Syndrome › nephritic

with edema

See: Nephrosis

Syndrome › nephritic

acute

N00.9

Syndrome › nephritic

chronic

N03.9

Syndrome › nephritic

rapidly progressive

N01.9

Syndrome

nephrotic(congenital)

N04.9

See also: Nephrosis

Syndrome › nephrotic(congenital)

with

Syndrome › nephrotic(congenital) › with

C3

Syndrome › nephrotic(congenital) › with › C3

glomerulonephritis

N04.A

Syndrome › nephrotic(congenital) › with › C3

glomerulopathy

N04.A

Syndrome › nephrotic(congenital) › with › C3 › glomerulopathy

with dense deposit disease

N04.6

Syndrome › nephrotic(congenital) › with

dense deposit disease

N04.6

Syndrome › nephrotic(congenital) › with

diffuse

Syndrome › nephrotic(congenital) › with › diffuse

crescentic glomerulonephritis

N04.7

Syndrome › nephrotic(congenital) › with › diffuse

endocapillary proliferative glomerulonephritis

N04.4

Syndrome › nephrotic(congenital) › with › diffuse

membranous glomerulonephritis

N04.20

Syndrome › nephrotic(congenital) › with › diffuse

mesangial proliferative glomerulonephritis

N04.3

Syndrome › nephrotic(congenital) › with › diffuse

mesangiocapillary glomerulonephritis

N04.5

Syndrome › nephrotic(congenital) › with

focal and segmental glomerular lesions

N04.1

Syndrome › nephrotic(congenital) › with

minor glomerular abnormality

N04.0

Syndrome › nephrotic(congenital) › with

specified morphological changes NEC

N04.8

Syndrome › nephrotic(congenital)

diabetic

See: Diabetes, nephrosis

Syndrome › nephrotic(congenital)

specified type NEC with diffuse membranous glomerulonephritis

N04.29

Syndrome

neurologic neglect

R41.4

Syndrome

Nonne-Milroy-Meige

Q82.0

Syndrome

Nothnagel's vasomotor acroparesthesia

I73.89

Syndrome

obesity hypoventilation(OHS)

E66.2

Syndrome

obliterans

Syndrome › obliterans

bronchiolitis

J44.81

See also: Bronchiolitis, obliterative

Syndrome

Oliver-McFarlane

Q87.89

Syndrome

ophthalmoplegia-cerebellar ataxia

See: Strabismus, paralytic, third nerve

Syndrome

oral-facial-digital

Q87.0

Syndrome

organic

Syndrome › organic

affective

F06.30

Syndrome › organic

amnesic(not alcohol- or drug-induced)

F04

Syndrome › organic

brain

F09

Syndrome › organic

depressive

F06.31

Syndrome › organic

hallucinosis

F06.0

Syndrome › organic

personality

F07.0

Syndrome

oro-facial-digital

Q87.0

Syndrome

Osler-Weber-Rendu

I78.0

Syndrome

osteoporosis-osteomalacia

M83.8

Syndrome

Osterreicher-Turner

Q87.2

Syndrome

otolith

Subcategory: H81.8

Syndrome

oto-palatal-digital

Q87.0

Syndrome

outlet(thoracic)

G54.0

See also: Syndrome, thoracic outlet

Syndrome

ovary

Syndrome › ovary

polycystic

E28.2

Syndrome › ovary

resistant

E28.39

Syndrome › ovary

sclerocystic

E28.2

Syndrome

pain

See also: Pain

Syndrome › pain

complex regional I

G90.50

Syndrome › pain › complex regional I

lower limb

G90.52-

Syndrome › pain › complex regional I

specified site NEC

G90.59

Syndrome › pain › complex regional I

upper limb

G90.51-

Syndrome › pain

complex regional II

See: Causalgia

Syndrome

painful

Syndrome › painful

bruising

D69.2

Syndrome › painful

feet

E53.8

Syndrome › painful

prostate

N42.81

Syndrome

paralysis agitans

See: Parkinsonism

Syndrome › paralytic

specified NEC

G83.89

Syndrome

parkinsonian

See: Parkinsonism

Syndrome

Parkinson's

See: Parkinsonism

Syndrome

paroxysmal facial pain

G50.0

Syndrome › Parry's

with thyroid storm

E05.01

Syndrome

Parsonage(-Aldren)-Turner

G54.5

Syndrome

Paterson(-Brown) (-Kelly)

D50.1

Syndrome

pectoralis minor

I77.89

Syndrome

pediatric acute-onset neuropsychiatric(PANS)

D89.89

Syndrome

pediatric autoimmune neuropsychiatric disorders associated with streptococcal infections(PANDAS)

D89.89

Syndrome

pediatric inflammatory multisystem

M35.81

Syndrome

pellagra-cerebellar ataxia-renal aminoaciduria

E72.02

Syndrome

pellagroid

E52

Syndrome

Pellegrini-Stieda

See: Bursitis, tibial collateral

Syndrome

pelvic congestion-fibrosis, female

N94.89

Syndrome

peptic ulcer

See: Ulcer, peptic

Syndrome

periodic fever

M04.1

Syndrome

periodic fever, aphthous stomatitis, pharyngitis, and adenopathy [PFAPA]

M04.8

Syndrome

periodic headache, in adults and children

See: Headache, periodic syndromes in adults and children

Syndrome

periurethral fibrosis

N13.5

Syndrome

phantom limb(without pain)

G54.7

Syndrome › phantom limb(without pain)

with pain

G54.6

Syndrome

pharyngeal pouch

D82.1

Syndrome

Pick's

See: Disease, Pick's

Syndrome

PIE(pulmonary infiltration with eosinophilia)

J82.89

See also: Eosinophilia, pulmonary

Syndrome

pigmentary pallidal degeneration(progressive)

G23.0

Syndrome

plantar fascia

M72.2-

Syndrome

placental transfusion

See: Pregnancy, complicated by, placental transfusion syndromes

Syndrome

plateau iris(post-iridectomy) (postprocedural)

H21.82

Syndrome

Plummer-Vinson

D50.1

Syndrome

pluricarential of infancy

E40

Syndrome

plurideficiency

E40

Syndrome

pluriglandular(compensatory)

E31.8

Syndrome › pluriglandular(compensatory)

autoimmune

E31.0

Syndrome

pneumatic hammer

T75.21

Syndrome

polyangiitis overlap

M30.8

Syndrome

polycarential of infancy

E40

Syndrome

polyglandular

E31.8

Syndrome › polyglandular

autoimmune

E31.0

Syndrome

popliteal

Syndrome › popliteal

artery entrapment

I77.89

Syndrome › popliteal

web

Q87.89

Syndrome

postbacterial fatigue

G93.39

Syndrome

postcardiac injury

Syndrome › postcardiac injury

postcardiotomy

I97.0

Syndrome › postcardiac injury

postmyocardial infarction

I24.1

Syndrome

postcardiotomy

I97.0

Syndrome

post chemoembolization - code to associated conditions

Syndrome

postcholecystectomy

K91.5